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510(k) Data Aggregation

K Number

Device Name

EUROMEDICAL REINFORCED ENDOTRACHEAL TUBE

Manufacturer

UNOMEDICAL SDN BHD

Date Cleared

1996-11-21

(154 days)

Product Code

Regulation Number

Type

Panel

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N/A

Why did this record match?

Device Name :

EUROMEDICAL REINFORCED ENDOTRACHEAL TUBE

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

Intended Use

Device Description

AI/ML Overview

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